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rph oct 2026

Last updated 1:23 AM on 9/12/26
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58 Terms

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<p>Monosubstituted benzene</p><p>a. Methylbenzene</p><p>b. Hydroxybenzene</p><p>c. Benzaldehyde&nbsp;</p><p>d. Aminobenzene&nbsp;</p>

Monosubstituted benzene

a. Methylbenzene

b. Hydroxybenzene

c. Benzaldehyde 

d. Aminobenzene 

d. Aminobenzene (Aniline) 

- assay: Diazotization

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<p>Monosubstituted benzene</p><p>a. Methylbenzene</p><p>b. Hydroxybenzene</p><p>c. Benzaldehyde&nbsp;</p><p>d. Aminobenzene&nbsp;</p>

Monosubstituted benzene

a. Methylbenzene

b. Hydroxybenzene

c. Benzaldehyde 

d. Aminobenzene 

a. Methylbenzene (Toluene)

-paint, thinners

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<p>Monosubstituted benzene</p><p>a. Methylbenzene</p><p>b. Hydroxybenzene</p><p>c. Benzaldehyde&nbsp;</p><p>d. Aminobenzene&nbsp;</p>

Monosubstituted benzene

a. Methylbenzene

b. Hydroxybenzene

c. Benzaldehyde 

d. Aminobenzene 

c. Benzaldehyde

-Synthetic Bitter Almond Oil

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<p>Disubstituted benzene </p><p>a. O-hydroxyphenol</p><p>b. O-hydroxybenzoic acid </p>

Disubstituted benzene

a. O-hydroxyphenol

b. O-hydroxybenzoic acid

a. O-hydroxyphenol/Catechol

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<p>Disubstituted benzene </p><p>a. O-hydroxyphenol</p><p>b. O-hydroxybenzoic acid </p>

Disubstituted benzene

a. O-hydroxyphenol

b. O-hydroxybenzoic acid

b. O-hydroxybenzoic acid (Salicyclic acid)

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<p>Poly-substituted benzenes</p><p>2,4,6-trinitrophenol is also known as:</p><p></p><p>a. lauric acid</p><p>b. acetic acid</p><p>c. picric acid</p><p></p>

Poly-substituted benzenes

2,4,6-trinitrophenol is also known as:


a. lauric acid

b. acetic acid

c. picric acid


c. picric acid

  • hager’s reagent active component

  • dry:explosive


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<p>Which Polycyclic aromatic carbons? </p><p>a. Anthracene</p><p>b. Pyrene</p><p>c. Naphthalene</p><p>d. Phenanthrene</p><p></p>

Which Polycyclic aromatic carbons?

a. Anthracene

b. Pyrene

c. Naphthalene

d. Phenanthrene


c. Naphthalene or mothballs

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<p>Which Polycyclic aromatic carbons? </p><p>a. Anthracene</p><p>b. Pyrene</p><p>c. Naphthalene</p><p>d. Phenanthrene</p>

Which Polycyclic aromatic carbons?

a. Anthracene

b. Pyrene

c. Naphthalene

d. Phenanthrene

d. Phenanthrene

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<p>Which Polycyclic aromatic carbons? </p><p>a. Anthracene</p><p>b. Pyrene</p><p>c. Naphthalene</p><p>d. Phenanthrene</p>

Which Polycyclic aromatic carbons?

a. Anthracene

b. Pyrene

c. Naphthalene

d. Phenanthrene

a. Anthracene

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<p>Which Polycyclic aromatic carbons? </p><p>a. Anthracene</p><p>b. Pyrene</p><p>c. Naphthalene</p><p>d. Phenanthrene</p>

Which Polycyclic aromatic carbons?

a. Anthracene

b. Pyrene

c. Naphthalene

d. Phenanthrene

b. Pyrene

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<p>Alcohol application to pharnacy. Identify the structure</p><p>a. Benzyl alcohol</p><p>b. Pyridoxine</p><p>c. Ascorbic acid</p><p>d. Tetracycline</p>

Alcohol application to pharnacy. Identify the structure

a. Benzyl alcohol

b. Pyridoxine

c. Ascorbic acid

d. Tetracycline

a. Benzyl alcohol

-also known as Phenylmethanol

-preservative in BWFI

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<p>Alcohol application to pharnacy. Identify the structure</p><p>a. Benzyl alcohol</p><p>b. Pyridoxine</p><p>c. Ascorbic acid</p><p>d. Tetracycline</p>

Alcohol application to pharnacy. Identify the structure

a. Benzyl alcohol

b. Pyridoxine

c. Ascorbic acid

d. Tetracycline

b. pyridoxine

  • Vitamin B6

  • Prophylaxis and Treatment for peripheral neuropathy


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<p>Alcohol application to pharnacy. Identify the structure</p><p>a. Benzyl alcohol</p><p>b. Pyridoxine</p><p>c. Ascorbic acid</p><p>d. Tetracycline</p>

Alcohol application to pharnacy. Identify the structure

a. Benzyl alcohol

b. Pyridoxine

c. Ascorbic acid

d. Tetracycline

c. Ascorbic acid

  • Vitamin C

  • Anti oxidant, Anti scurvy

  • Least stable vitamin


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<p>Alcohol application to pharnacy. Identify the structure</p><p>a. Benzyl alcohol</p><p>b. Pyridoxine</p><p>c. Ascorbic acid</p><p>d. Tetracycline</p>

Alcohol application to pharnacy. Identify the structure

a. Benzyl alcohol

b. Pyridoxine

c. Ascorbic acid

d. Tetracycline

d. Tetracycline

  • Antibacterial agent


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<p>Alcohol application to pharnacy. Identify the structure</p><p>a. Menthol</p><p>b. Terpin hydrates</p><p>c. Glycerol</p><p>d. Sorbitol </p>

Alcohol application to pharnacy. Identify the structure

a. Menthol

b. Terpin hydrates

c. Glycerol

d. Sorbitol

a. Menthol

  • Flavorant


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<p>Alcohol application to pharnacy. Identify the structure</p><p>a. Menthol</p><p>b. Terpin hydrates</p><p>c. Glycerol</p><p>d. Sorbitol </p>

Alcohol application to pharnacy. Identify the structure

a. Menthol

b. Terpin hydrates

c. Glycerol

d. Sorbitol

c. Glycerol

  • Humectant - remain moisture


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<p>Alcohol application to pharnacy. Identify the structure</p><p>a. Menthol</p><p>b. Terpin hydrates</p><p>c. Glycerol</p><p>d. Sorbitol</p>

Alcohol application to pharnacy. Identify the structure

a. Menthol

b. Terpin hydrates

c. Glycerol

d. Sorbitol

b. Terpin hydrates

  • Terpinols

  • Expectorant


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<p>Alcohol application to pharnacy. Identify the structure</p><p>a. Menthol</p><p>b. Terpin hydrates</p><p>c. Glycerol</p><p>d. Sorbitol</p>

Alcohol application to pharnacy. Identify the structure

a. Menthol

b. Terpin hydrates

c. Glycerol

d. Sorbitol

d. Sorbitol

  • Glucitol

  • Humectant- toothpaste


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<p>Example of phenol. Identify the ff structure</p><p>a. Resorcinol</p><p>b. Benzene -1,2- diol</p><p>c. Benzene-1,3-diol</p><p>d. a and c</p>

Example of phenol. Identify the ff structure

a. Resorcinol

b. Benzene -1,2- diol

c. Benzene-1,3-diol

d. a and c

d. a and c


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<p>Example of phenol. Identify the ff structure</p><p>a. Hydroquinone</p><p>b. Thymol</p><p>c. Eugenol</p><p>d. Resorcinol</p>

Example of phenol. Identify the ff structure

a. Hydroquinone

b. Thymol

c. Eugenol

d. Resorcinol

a. Hydroquinone

  • Depigmenting agent


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<p>Example of phenol. Identify the ff structure</p><p>a. Thymol</p><p>b. Eugenol</p><p>c. 4-allyl-2-methoxy phenol</p><p>d. Resorcinol</p>

Example of phenol. Identify the ff structure

a. Thymol

b. Eugenol

c. 4-allyl-2-methoxy phenol

d. Resorcinol

a. Thymol

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<p>Example of phenol. Identify the ff structure</p><p>a. Thymol</p><p>b. Hydroquinone</p><p>c. Catechol</p><p>d. Eugenol</p>

Example of phenol. Identify the ff structure

a. Thymol

b. Hydroquinone

c. Catechol

d. Eugenol

d. Eugenol

  • source: clove oil, eugenia caryophyllus


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<p>Phenol Application to pharmacy</p><p>a. Gingerol</p><p>b. Hesperidin</p><p>c. Vanillin</p>

Phenol Application to pharmacy

a. Gingerol

b. Hesperidin

c. Vanillin

b. Hesperidin

  • flavonoid polyphenolic glycoside

  • test: Ferric chloride/fecl3


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<p>Phenol Application to pharmacy</p><p>a. Gingerol</p><p>b. Hesperidin</p><p>c. Vanillin</p>

Phenol Application to pharmacy

a. Gingerol

b. Hesperidin

c. Vanillin

a. Gingerol

  • Oleoresin


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<p>Ether application to pharmacy. Identify the ff structure</p><p>a. Sorbitol</p><p>b. Eugenol</p><p>c. Thymol</p><p>d. Eucalyptol</p>

Ether application to pharmacy. Identify the ff structure

a. Sorbitol

b. Eugenol

c. Thymol

d. Eucalyptol

d. Eucalyptol

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<p>Aldehyde application to pharmacy</p><p>a. Acrolein</p><p>b. Vanillin</p><p>c. Hesperidin</p><p>d. Curcumin</p>

Aldehyde application to pharmacy

a. Acrolein

b. Vanillin

c. Hesperidin

d. Curcumin

b. Vanillin

  • 4-hydroxy-3-methoxybenzaldehyde

  • Flavorant, Anti inflammatory agent


<p>b. Vanillin</p><ul><li><p>4-hydroxy-3-methoxybenzaldehyde</p></li><li><p>Flavorant, Anti inflammatory agent</p></li></ul><p></p>
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<p>Aldehyde application to pharmacy</p><p>a. Acrolein</p><p>b. Vanillin</p><p>c. Hesperidin</p><p>d. Curcumin</p>

Aldehyde application to pharmacy

a. Acrolein

b. Vanillin

c. Hesperidin

d. Curcumin

a. Acrolein

  • causes Hemorrhagic Cystisis


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<p>Ketone Application to Pharmacy. Identify the ff structure</p><p>a. Cocaine</p><p>b. Valproic acid</p><p>c. Haloperidol</p><p>d. Methylsalicylate</p>

Ketone Application to Pharmacy. Identify the ff structure

a. Cocaine

b. Valproic acid

c. Haloperidol

d. Methylsalicylate

c. Haloperidol

  • antipsychotic

  • butyrophenone derivative (peridol)


<p>c. Haloperidol</p><ul><li><p>antipsychotic</p></li><li><p>butyrophenone derivative (peridol)</p></li></ul><p></p>
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<p>Benzoic Acid Derivatives or Ester Local Anesthetic. Identify the ff structure</p><p>a. Benzocaine</p><p>b. Cocaine</p><p>c. Procaine</p>

Benzoic Acid Derivatives or Ester Local Anesthetic. Identify the ff structure

a. Benzocaine

b. Cocaine

c. Procaine

b. Cocaine

-Methyl ester of benzoylecgonine

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<p>Benzoic Acid Derivatives or Ester Local Anesthetic. Identify the ff structure</p><p>a. Benzocaine</p><p>b. Cocaine</p><p>c. Procaine</p>

Benzoic Acid Derivatives or Ester Local Anesthetic. Identify the ff structure

a. Benzocaine

b. Cocaine

c. Procaine

c. Procaine

  • 2-diethylaminoethyl ester of 4-aminobenzoic acid


<p>c. Procaine</p><ul><li><p>2-diethylaminoethyl ester of 4-aminobenzoic acid</p></li></ul><p></p>
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<p>Benzoic Acid Derivatives or Ester Local Anesthetic. Identify the ff structure</p><p>a. Benzocaine</p><p>b. Cocaine</p><p>c. Procaine</p>

Benzoic Acid Derivatives or Ester Local Anesthetic. Identify the ff structure

a. Benzocaine

b. Cocaine

c. Procaine

a. Benzocaine

  • ethyl ester of

    4-aminobenzoic acid


<p>a. Benzocaine</p><ul><li><p>ethyl ester of</p><p class="p1">4-aminobenzoic acid</p></li></ul><p></p>
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<p>Benzoic Acid Derivatives or Ester Local Anesthetic application to pharmacy. Identify the ff structure</p><p>a. Valproic acid</p><p>b. Prostaglandins</p><p>c. Citric acid</p><p>d. Salicylic acid</p>

Benzoic Acid Derivatives or Ester Local Anesthetic application to pharmacy. Identify the ff structure

a. Valproic acid

b. Prostaglandins

c. Citric acid

d. Salicylic acid

d. Salicylic acid

  • also knon as O-hydroxybenzoic acid

  • 2-hydroxybenzoic acid

  • keratolytic agent


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<p>Benzoic Acid Derivatives or Ester Local Anesthetic application to pharmacy. Identify the ff structure</p><p>a. Valproic acid</p><p>b. Prostaglandins</p><p>c. Citric acid</p><p>d. Salicylic acid</p>

Benzoic Acid Derivatives or Ester Local Anesthetic application to pharmacy. Identify the ff structure

a. Valproic acid

b. Prostaglandins

c. Citric acid

d. Salicylic acid

b. Prostaglandins

  • from arachidonic acid

  • hormone like-autacoids but closely resembles lipids


<p>b. Prostaglandins</p><ul><li><p>from arachidonic acid</p></li><li><p>hormone like-autacoids but closely resembles lipids</p></li></ul><p></p>
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<p>Benzoic Acid Derivatives or Ester Local Anesthetic application to pharmacy. Identify the ff structure</p><p>a. Valproic acid</p><p>b. Prostaglandins</p><p>c. Citric acid</p><p>d. Salicylic acid</p>

Benzoic Acid Derivatives or Ester Local Anesthetic application to pharmacy. Identify the ff structure

a. Valproic acid

b. Prostaglandins

c. Citric acid

d. Salicylic acid

a. Valproic acid

  • 2-propylpentanoic acid

  • -antiepileptic, antisseizure


<p>a. Valproic acid</p><ul><li><p>2-propylpentanoic acid</p></li><li><p>-antiepileptic, antisseizure</p></li></ul><p></p>
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<p>Benzoic Acid Derivatives or Ester Local Anesthetic application to pharmacy. Identify the ff structure</p><p>a. Valproic acid</p><p>b. Prostaglandins</p><p>c. Citric acid</p><p>d. Salicylic acid</p>

Benzoic Acid Derivatives or Ester Local Anesthetic application to pharmacy. Identify the ff structure

a. Valproic acid

b. Prostaglandins

c. Citric acid

d. Salicylic acid

c. Citric acid

  • promotes dissolution of fentanyl into saliva- increase analgesic potency of buccal tablets


<p>c. Citric acid</p><ul><li><p>promotes dissolution of fentanyl into saliva- increase analgesic potency of buccal tablets</p></li></ul><p></p>
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<p>Application to pharmacy of Esters. identify the ff structure</p><p>a. Cocaine</p><p>b. Triglycerides/fats</p><p>c. Benzocaine</p><p>d, Procaine</p>

Application to pharmacy of Esters. identify the ff structure

a. Cocaine

b. Triglycerides/fats

c. Benzocaine

d, Procaine

b. Triglycerides/fats

  • Esters of glycerin and fatty acids


<p>b. Triglycerides/fats</p><ul><li><p>Esters of glycerin and fatty acids</p></li></ul><p></p>
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<p>Phenothiazine Derivatives (Antipsychotic Drugs)</p><p>Aliphatic side chain</p>

Phenothiazine Derivatives (Antipsychotic Drugs)

Aliphatic side chain

CHLORPROMAZINE

<p>CHLORPROMAZINE</p>
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<p>Phenothiazine Derivatives (Antipsychotic Drugs)</p><p>Aliphatic side chain</p>

Phenothiazine Derivatives (Antipsychotic Drugs)

Aliphatic side chain

PROMAZINE

<p>PROMAZINE</p>
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<p>a. tranylcypromine</p><p>b. phenylpropanolamine</p><p>c. acetaminophen</p>

a. tranylcypromine

b. phenylpropanolamine

c. acetaminophen

a. tranylcypromine

  • nonselective mao inhibitor

  • antidepressant


<p>a. tranylcypromine</p><ul><li><p>nonselective mao inhibitor</p></li><li><p>antidepressant</p></li></ul><p></p>
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<p>a. tranylcypromine</p><p>b. phenylpropanolamine</p><p>c. acetaminophen</p>

a. tranylcypromine

b. phenylpropanolamine

c. acetaminophen

c. acetaminophen

  • aniline derivative


<p>c. acetaminophen</p><ul><li><p>aniline derivative</p></li></ul><p></p>
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<p>What alkaloid is this?</p><p>a. Atropine</p><p>b. Digoxin</p><p>c. Quinine</p><p>d. Colchicine</p>

What alkaloid is this?

a. Atropine

b. Digoxin

c. Quinine

d. Colchicine

c. Quinine

  • Quinine sulphate may be dissolved in water by addition of

    a small amount of sulphuric acid to convert it to more

    soluble bisulfate.

    Application to Pharmac


<p>c. Quinine</p><ul><li><p>Quinine sulphate may be dissolved in water by addition of</p><p class="p1">a small amount of sulphuric acid to convert it to more</p><p class="p1">soluble bisulfate.</p><p class="p1">Application to Pharmac</p></li></ul><p></p>
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<p>Application of Amide Local Anesthetics. Identify the ff structure. </p><p>a. Lidocaine</p><p>b. Bupivacaine</p><p>c. Procaine</p><p>d. Dibucaine </p>

Application of Amide Local Anesthetics. Identify the ff structure.

a. Lidocaine

b. Bupivacaine

c. Procaine

d. Dibucaine

a. Lidocaine

  • Xylocaine (brand name)

  • Esterases/Amidases


<p>a. Lidocaine</p><ul><li><p>Xylocaine (brand name) </p></li><li><p>Esterases/Amidases</p></li></ul><p></p>
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<p>Monobactam aka “magic bullet” for Pseudomonas</p><p>a. Vancomycin</p><p>b. Thienamycin</p><p>c. Imipenem</p><p>d. Aztreonam</p>

Monobactam aka “magic bullet” for Pseudomonas

a. Vancomycin

b. Thienamycin

c. Imipenem

d. Aztreonam

d. Aztreonam

  • has 4 methyl group that increased stability of monobactam to B lactamase and increased activity against gram negative bacteria


<p>d. Aztreonam</p><ul><li><p>has 4 methyl group that increased stability of monobactam to B lactamase and increased activity against gram negative bacteria</p></li></ul><p></p>
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